Fort Lauderdale, FL · On-site
$19 - $20/hr
The ideal candidate is bilingual (English/Spanish) , organized, and has prior experience in pharmaceutical or FDA-regulated environments. Location: Miramar, FL Industry: Pharmaceutical Manufacturing ...
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Fort Lauderdale, FL · On-site
$19 - $20/hr
The ideal candidate is bilingual (English/Spanish) , organized, and has prior experience in pharmaceutical or FDA-regulated environments. Location: Miramar, FL Industry: Pharmaceutical Manufacturing ...
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Melbourne, FL · On-site
This role is responsible for ensuring products are manufactured, tested, and released in compliance with FDA regulations, Good Manufacturing Practices (GMP), and internal quality standards. The ideal ...
New
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Melbourne, FL · On-site
This role is responsible for ensuring products are manufactured, tested, and released in compliance with FDA regulations, Good Manufacturing Practices (GMP), and internal quality standards. The ideal ...
New
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Melbourne, FL · On-site
This role is responsible for ensuring products are manufactured, tested, and released in compliance with FDA regulations, Good Manufacturing Practices (GMP), and internal quality standards. The ideal ...
New
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Melbourne, FL · On-site
This role is responsible for ensuring products are manufactured, tested, and released in compliance with FDA regulations, Good Manufacturing Practices (GMP), and internal quality standards. The ideal ...
New
West Palm Beach, FL · On-site
$18 - $24/hr
Position Summary The QA Technician ensures that all raw materials, in-process production, and finished products meet quality and food safety standards (GMP, SQF, FDA). This role is essential in ...
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West Palm Beach, FL · On-site
$18 - $24/hr
Position Summary The QA Technician ensures that all raw materials, in-process production, and finished products meet quality and food safety standards (GMP, SQF, FDA). This role is essential in ...
Fort Lauderdale, FL · On-site
$19/hr
The ideal candidate is bilingual (English/Spanish) , organized, and has prior experience in pharmaceutical or FDA-regulated environments. Location: Miramar, FL Industry: Pharmaceutical Manufacturing ...
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Fort Lauderdale, FL · On-site
$19/hr
The ideal candidate is bilingual (English/Spanish) , organized, and has prior experience in pharmaceutical or FDA-regulated environments. Location: Miramar, FL Industry: Pharmaceutical Manufacturing ...
Maintain compliance with Good Manufacturing Practices (GMP), FDA regulations, and company safety policies. * Keep maintenance tools, equipment, and work areas clean and organized. * Respond quickly ...
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Maintain compliance with Good Manufacturing Practices (GMP), FDA regulations, and company safety policies. * Keep maintenance tools, equipment, and work areas clean and organized. * Respond quickly ...
Miami Lakes, FL · On-site
$50K - $65K/yr
Customs, FDA, USDA and other relevant government agencies. * Correctly classify cargo using the Harmonized Tariff Schedule (HTS). * Explain classifications to customers in a clear, understandable ...
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Miami Lakes, FL · On-site
$50K - $65K/yr
Customs, FDA, USDA and other relevant government agencies. * Correctly classify cargo using the Harmonized Tariff Schedule (HTS). * Explain classifications to customers in a clear, understandable ...
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Miramar, FL · On-site
$30/hr
Maintain compliance with Good Manufacturing Practices (GMP), FDA regulations, and company safety policies. * Keep maintenance tools, equipment, and work areas clean and organized. * Respond quickly ...
New
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Miramar, FL · On-site
$30/hr
Maintain compliance with Good Manufacturing Practices (GMP), FDA regulations, and company safety policies. * Keep maintenance tools, equipment, and work areas clean and organized. * Respond quickly ...
New
Knowledge in cGMP regulations and FDA guidelines * Detailed oriented * Basic computer and math skills.
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Knowledge in cGMP regulations and FDA guidelines * Detailed oriented * Basic computer and math skills.
Miami, FL · On-site
$155K - $180K/yr
If you thrive in a fast-paced clinical research environment and enjoy leading teams, overseeing study execution, and ensuring compliance with FDA, ICH, and GCP guidelines, this could be your next ...
New
Miami, FL · On-site
$155K - $180K/yr
If you thrive in a fast-paced clinical research environment and enjoy leading teams, overseeing study execution, and ensuring compliance with FDA, ICH, and GCP guidelines, this could be your next ...
New
Tampa, FL · On-site
Lead the overall Quality Management System and ensure compliance with FDA Quality Management System Regulation (QMSR), ISO 13485, ISO 14971, and other applicable requirements. * Build strong ...
Tampa, FL · On-site
Lead the overall Quality Management System and ensure compliance with FDA Quality Management System Regulation (QMSR), ISO 13485, ISO 14971, and other applicable requirements. * Build strong ...
Naples, FL · On-site
$140 - $210/hr
Quality System Leadership Lead and oversee the end-to-end QMS, ensuring compliance with FDA, ISO 13485, and global regulatory requirements Establish and drive quality strategy, governance, and system ...
New
Naples, FL · On-site
$140 - $210/hr
Quality System Leadership Lead and oversee the end-to-end QMS, ensuring compliance with FDA, ISO 13485, and global regulatory requirements Establish and drive quality strategy, governance, and system ...
New
$41 - $56/hr
Ensure compliance with FDA regulations, Good Clinical Practice (GCP), IRB requirements, and sponsor guidelines. * Develop and implement operational processes to improve efficiency and quality.
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$41 - $56/hr
Ensure compliance with FDA regulations, Good Clinical Practice (GCP), IRB requirements, and sponsor guidelines. * Develop and implement operational processes to improve efficiency and quality.
$100K - $150K/yr
We are seeking an experienced Quality Assurance & Compliance Manager to lead the Quality function within an FDA-regulated medical device manufacturing environment. This individual will be responsible ...
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$100K - $150K/yr
We are seeking an experienced Quality Assurance & Compliance Manager to lead the Quality function within an FDA-regulated medical device manufacturing environment. This individual will be responsible ...
Miramar, FL · On-site
$18/hr
Knowledge in cGMP regulations and FDA guidelines * Detailed oriented * Basic computer and math skills.
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Miramar, FL · On-site
$18/hr
Knowledge in cGMP regulations and FDA guidelines * Detailed oriented * Basic computer and math skills.
Doral, FL · On-site
Ensure compliance with FDA, USDA, HACCP, GMP, SOP, and SSOP requirements. * Conduct plant, pre-operational, raw material, and internal inspections. * Train employees on sanitation procedures, GMPs ...
Doral, FL · On-site
Ensure compliance with FDA, USDA, HACCP, GMP, SOP, and SSOP requirements. * Conduct plant, pre-operational, raw material, and internal inspections. * Train employees on sanitation procedures, GMPs ...
... FDA and global regulatory authorities • Ensure compliance with GxP, 21 CFR Part 11, HIPAA, and ICH E6 guidelines Data Engineering & Automation • Architect and implement end-to-end clinical data ...
... FDA and global regulatory authorities • Ensure compliance with GxP, 21 CFR Part 11, HIPAA, and ICH E6 guidelines Data Engineering & Automation • Architect and implement end-to-end clinical data ...
$55K - $71K/yr
To prepares and maintain FDA applications for Investigational New Drugs (INDs) and Investigational Device Exemptions (IDEs). * To lead the implementation of study specific regulatory processes of a ...
$55K - $71K/yr
To prepares and maintain FDA applications for Investigational New Drugs (INDs) and Investigational Device Exemptions (IDEs). * To lead the implementation of study specific regulatory processes of a ...
Quality System Leadership Lead and oversee the end-to-end QMS, ensuring compliance with FDA, ISO 13485, and global regulatory requirements Establish and drive quality strategy, governance, and system ...
Quality System Leadership Lead and oversee the end-to-end QMS, ensuring compliance with FDA, ISO 13485, and global regulatory requirements Establish and drive quality strategy, governance, and system ...
Serve as Principal Investigator or Sub-Investigator on FDA form 1572 for protocols conducted. * Satisfactorily perform and comply with all responsibilities of a clinical investigator including, but ...
Serve as Principal Investigator or Sub-Investigator on FDA form 1572 for protocols conducted. * Satisfactorily perform and comply with all responsibilities of a clinical investigator including, but ...
| Aspect | Fda Job | Food Scientist |
|---|---|---|
| Required Credentials | Bachelor's degree in life sciences, regulatory affairs, or related field; sometimes advanced degrees | Bachelor's or master's in food science, microbiology, or chemistry |
| Work Environment | Regulatory agencies, laboratories, inspection sites | Food manufacturing facilities, laboratories, research settings |
| Industry Usage | Government regulatory body overseeing food safety | Private sector food companies, research institutions |
| Common Search/Comparison | Fda Job vs Food Scientist | Food Scientist roles and responsibilities |
Fda Jobs primarily focus on regulatory compliance, inspections, and policy enforcement within government agencies. Food Scientists, on the other hand, work in research and development, product testing, and improving food safety in private or academic sectors. While both roles involve food safety, Fda Jobs are centered on regulation and oversight, whereas Food Scientists focus on innovation and product quality.
$19 - $20/hr
Full-time
Re-posted 25 days ago
A well-established pharmaceutical company in Miramar, FL is seeking an experienced and detail-oriented Quality Assurance (QA) Document Control Specialist to support its evening shift operations. This role is responsible for maintaining, reviewing, and managing GMP documentation to ensure compliance with regulatory standards. The ideal candidate is bilingual (English/Spanish), organized, and has prior experience in pharmaceutical or FDA-regulated environments.
Location: Miramar, FL
Industry: Pharmaceutical Manufacturing
Job Type: Full-Time
Schedule: Monday to Friday, 2:30 PM – 11:00 PM
Pay: $19.00 per hour
Maintain and control quality documentation in accordance with GMP and FDA guidelines
Review and archive manufacturing, packaging, and testing records for accuracy and completeness
Ensure proper version control and distribution of controlled documents (SOPs, batch records, etc.)
Assist in audits, inspections, and internal reviews by preparing and providing requested documentation
Support QA team in implementing document changes, updates, and approvals
Ensure timely and accurate entry of documentation into digital or physical filing systems
Collaborate with production, quality, and regulatory departments to ensure documentation compliance
Report any deviations or non-conformances found in records
Minimum 1–2 years of experience in document control or QA in a pharmaceutical or FDA-regulated environment
High school diploma or equivalent required; associate or bachelor's degree preferred
Strong knowledge of GMP, SOPs, and document control best practices
Excellent attention to detail and organizational skills
Bilingual (English/Spanish) – required
Proficient in Microsoft Office (Excel, Word, Outlook)
Ability to work independently with minimal supervision during evening shift hours
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